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EP0141327B2 - Hydrosoluble copolymers and their use as dispersants of solid matter - Google Patents
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EP0141327B2 - Hydrosoluble copolymers and their use as dispersants of solid matter - Google Patents

Hydrosoluble copolymers and their use as dispersants of solid matter Download PDF

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Publication number
EP0141327B2
EP0141327B2 EP84112373A EP84112373A EP0141327B2 EP 0141327 B2 EP0141327 B2 EP 0141327B2 EP 84112373 A EP84112373 A EP 84112373A EP 84112373 A EP84112373 A EP 84112373A EP 0141327 B2 EP0141327 B2 EP 0141327B2
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meth
ammonium
acrylamide
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German (de)
French (fr)
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EP0141327A1 (en
EP0141327B1 (en
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Martin Dr. Hille
Wolfgang Friede
Heinz Wittkus
Friedrich Dr. Engelhardt
Ulrich Riegel
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Hoechst AG
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Hoechst AG
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    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B24/00Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
    • C04B24/16Sulfur-containing compounds
    • C04B24/161Macromolecular compounds comprising sulfonate or sulfate groups
    • C04B24/163Macromolecular compounds comprising sulfonate or sulfate groups obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F228/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a bond to sulfur or by a heterocyclic ring containing sulfur
    • C08F228/02Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a bond to sulfur or by a heterocyclic ring containing sulfur by a bond to sulfur
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/02Well-drilling compositions
    • C09K8/04Aqueous well-drilling compositions
    • C09K8/14Clay-containing compositions
    • C09K8/18Clay-containing compositions characterised by the organic compounds
    • C09K8/22Synthetic organic compounds
    • C09K8/24Polymers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/42Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
    • C09K8/46Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement

Definitions

  • the present invention relates to copolymers as dispersants for solids in preferably aqueous solution.
  • the nature of the solids can be very different and their concentrations in the liquid phase fluctuate greatly.
  • the process according to the invention disperses solids in concentrations of a few mg / l just as effectively as in solids-rich systems, e.g. Drilling fluids, mineral binders such as cement and gypsum slurries, kaolin, coal, calcium carbonate sludges, etc., sometimes with extremely low solvent contents.
  • the process according to the invention enables the water content to be minimized and the viscosity to be reduced, which offers technical advantages.
  • dispersions such as drilling fluids, cement slurries, coal slurries, pesticide and pigment dispersions, etc.
  • dispersing agents are used to optimize the properties.
  • dispersants are used e.g. Polyphosphates, quebracho and especially lignol sulfonates and lignites e.g. according to DAS 1183 874.
  • copolymers of styrene sulfonate and maleic anhydride according to US Pat. No. 3,730,900 have found their way into the drilling fluid technology as liquefiers for high temperatures.
  • copolymers of vinyl sulfonate and vinyl amide in accordance with DOS 2 931 897 and DAS 2 444 108 have proven themselves very well when used in saline drilling fluids to stabilize pre-set properties in very deep hot holes.
  • dispersants reduce the viscosity. This facilitates the pumping process and allows the water content to be reduced, which improves the mechanical properties of the hardened concrete.
  • Lignosulfonates, polyacrylic acids, condensation products of mononaphthalenesulfonates and formaldehyde according to US Pat. No. 3,465,825 and N-sulfoalkyl-substituted acrylamides according to US Pat. No. 4,053,323 are used as dispersants in cement slurries.
  • cement slurries are added with water loss reducers, setting retarders or setting accelerators, which must be compatible with the respective dispersant. This limits the usability of the dispersant types. For example, When using calcium salts as setting accelerators, no polyacrylic acids are used as dispersing agents.
  • Partially saponified polyacrylamides as water void reducers also decrease significantly in their presence in the presence of calcium chloride. At particularly high loads on the dispersions e.g. cement slurries and drilling fluids based on salt water for very deep and hot drilling, it is difficult to set optimal properties.
  • copolymers of (meth) acrylamidoalkylsulfonic acids and (meth) acrylamide as drilling aids (US-A4 293 427).
  • DE-B 2 444 108 discloses the use of a copolymer which consists of vinyl or alkylsulfonic acids, (meth) acrylamides and N-vinyl-N-alkylcarbonamides.
  • non-, cationic and cationic surfactants are also used as dispersants.
  • the invention relates to the use of copolymers consisting of 5-95% by weight of (meth) acrylic acid or its ammonium or alkali salts or partially saponified (meth) acrylamide and 5-95% by weight of groups of the formula II, III, or IV wherein R 3 is hydrogen, C 1 -C s -alkyl or phenyl and R 4 is a hydrogen atom or CH 3 and R 5 are C 1 -C 10 -alkylene and K + ammonium, lithium, sodium or potassium, with the exception of those copolymers consisting of hydrolyzed acrylamide and 2-acrylamido-2-methylpropanesulfonic acid or consist of acrylamide or acrylic acid and ethylene sulfonate, as a dispersant in cement slurries and drilling fluids.
  • the molecular weights of the copolymers are between 2,000 and 6 million, preferably between 10,000 and 500,000. Higher molecular weights are required in the event of extreme demands on the suspension, such as high temperatures and salinity levels and low water emissions.
  • the copolymers to be used can be prepared in a manner known per se by reacting the monomers at temperatures between about -10 and + 80 ° C., preferably at 20 to 60 ° C., in the presence of suitable polymerization catalysts.
  • the polymerization is expediently carried out in the aqueous phase; however, aqueous solutions of water-miscible organic solvents, such as e.g. Methanol, ethanol, tert. Butyl alcohol, tetrahydrofuran or dimethylformamide serve as the polymerization medium.
  • Per-compounds such as benzoyl peroxide, acetyl peroxide, tert.
  • cocatalysts such as dibutylamine hydrochloride or traces of copper salts may also be appropriate.
  • Compounds such as e.g. Diazoisobutyronitrile can be added.
  • the mixed polymrisates are obtained as viscous, preferably aqueous solutions. They can be used in this form. If it is intended to prepare the copolymers in solid form, the polymer solutions can be subjected to an evaporation or drying process, e.g. Spray or roller drying. For the application, it makes sense that the sulfo groups are present in the copolymers in the form of the ammonium or alkali salts.
  • the copolymers have a very effective dispersing effect on very small amounts of solids, e.g. Calcium carbonate in technical cooling circuits of only e.g. 10 ppm or up to 80% solids content in cement slurries with a high solids content.
  • the minimum application concentration in the cooling water is 5 ppm, while it can be up to 20% in the cement slurry.
  • the high concentrations in the cement slurries noticeably improve the mechanical properties of the hardened cement. Only the very good dispersing effect of the copolymers makes it possible to homogeneously distribute the high concentrations of these polymers mentioned in the cement slurry.
  • a slurry of freshly precipitated calcium carbonate (100 mg / l) in water was used. 500 ml of this slurry were added in measuring cylinders 25, 100 and 500 ppm of a copolymer consisting of 10% methallylsulfonic acid and 90% acrylic acid (K value approx. 30). It was shaken for about 2 hours left to stand, then decant the above amount of water (250 m 3 ) and determine the solids content therein.
  • Copolymers A A:
  • the drilling fluids were measured at 20 ° C and then after aging for 15 hours at 200 ° C.
  • the K value the polymer (Fikentscher, Cellulose-Chemie 13, 1932, p. 58) was approx. 60 for the polymers.
  • the apparent viscosity and the yield point were measured with the FANN viscometer 35 SA.
  • the water loss according to API is the filtration rate in 30 minutes according to «API Code 29» with a standardized filter press at 7 kg / cm 2 .
  • the amount of the copolymers used is 0.75% in each case. Apparent viscosity and yield point were determined with the FANN 35 SA viscometer.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Ceramic Engineering (AREA)
  • Dispersion Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Medicinal Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Structural Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Soil Conditioners And Soil-Stabilizing Materials (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

For the Contracting states BE, CH, DE, FR, GB, IT, LI, NL 1. A copolymer consisting of-9-95 % by weight of (meth)acrylic acid or ammonium or alkali metal salts thereof or partly hydrolysed (meth)acrylamide and of 5-95 % by weight of groups of the formula II, III or IV see diagramm : EP0141327,P6,F1 in which R**3 denotes hydrogen, C1 -C6 -alkyl or phenyl, R**4 denotes a hydrogen atom or CH3 , and R**5 denotes C1 -C10 -alkylene and K**+ denotes ammonium, lithium, sodium or potassium For the Contracting state AT 1. A process for the preparation of a copolymer consisting of 5-95 % by weight of (meth)acrylic acid or ammonium or alkali metal salts thereof or partly hydrolysed (meth)acrylamide and of 5-95 % by weight of groups of the formula II, III ou IV see diagramm : EP0141327,P6,F1 in which R**3 denotes hydrogen, C1 -C6 -alkyl or phenyl, R**4 denotes a hydrogen atom or CH3 , and R**5 denotes C1 -C10 -alkylene and K**+ denotes ammonium, lithium, sodium or potassium, characterized in that (meth)acrylic acid or ammonium or alkali metal salts thereof partly hydrolysed (meth)-acrylamide and the definitely unsaturated monomers on which the formulae II-IV are based are polymerized in the stated proportions.

Description

Die vorliegende Erfindung betrifft Mischpolymerisate als Dispergatoren für Feststoffe in vorzugsweise wäßriger Lösung. Dabei kann die Natur der Feststoffe sehr unterschiedlich sein und deren Konzentrationen in der flüssigen Phase sehr stark schwanken. So werden durch das erfindungsgemäße Verfahren Feststoffe in Konzentrationen von wenigen mg/I ebenso wirkungsvoll dispergiert wie auch in feststoffreichen Systemen z.B. Bohrspülungen, mineralischen Bindern wie Zement- und Gipsschlämme, Kaolin-, Kohle-, Kalziumkarbonatschlämmen usw. mit teilweise extrem niedrigen Lösemittelgehalten. Bei den hochkonzentrierten Feststoffdispersionen ermöglicht das erfindungsgemäße Verfahren eine Minimierung des Wassergehaltes und eine Reduktion der Viskosität, was technische Vorteile bietet.The present invention relates to copolymers as dispersants for solids in preferably aqueous solution. The nature of the solids can be very different and their concentrations in the liquid phase fluctuate greatly. For example, the process according to the invention disperses solids in concentrations of a few mg / l just as effectively as in solids-rich systems, e.g. Drilling fluids, mineral binders such as cement and gypsum slurries, kaolin, coal, calcium carbonate sludges, etc., sometimes with extremely low solvent contents. In the case of the highly concentrated solid dispersions, the process according to the invention enables the water content to be minimized and the viscosity to be reduced, which offers technical advantages.

Für die verschiedensten Dispersionen wie Bohrspülungen, Zementschlämme, Kohleaufschlämmungen, Pestizid- und Farbpigmentdispersionen usw. werden zur Optimierung der Eigenschaften sehr unterschiedliche Dispergierhilfsmittel eingesetzt.For a wide variety of dispersions such as drilling fluids, cement slurries, coal slurries, pesticide and pigment dispersions, etc., very different dispersing agents are used to optimize the properties.

In Bohrspülungen verwendet man als Dispergatoren z.B. Polyphosphate, Quebracho und besonders Lignolsulfonate und Lignite z.B. gemäß DAS 1183 874. In neuerer Zeit haben als Verflüssiger für hohe Temperaturen Copolymere aus Styrolsulfonat und Maleinsäureanhydrid gemäß US Patent Nr. 3 730 900 Eingang in die Bohrspültechnik gefunden.In drilling fluids, dispersants are used e.g. Polyphosphates, quebracho and especially lignol sulfonates and lignites e.g. according to DAS 1183 874. Recently, copolymers of styrene sulfonate and maleic anhydride according to US Pat. No. 3,730,900 have found their way into the drilling fluid technology as liquefiers for high temperatures.

Muß für Bohrspülungen salines Wasser beim Durchbohren von Salzformationen oder beim Bohren auf offenem Meer verwendet werden, dann sind zur Stabilisierung dieser Dispersionen Schutzkolloide wie Stärke und Stärkederivate, Carboximethylhydroxiethyl-carboxymethylcellulosen, Biopolymere und teilverseifte Acrylamide notwendig. Bei sehr hohen Feststoffgehalten werden niedermolekulare ionische Polymere bevorzugt. Der Einsatz der Additive für Bohrspülungen ist sehr ausführlich in: George R. Gray, H.C.H. Darly, Walter F. Rogers « Composition and Properties of Oil Well Drilling Fluids, Fourth Edition, Gulf Publishing Company Houston/Texas 1980 » beschrieben.If saline water has to be used for drilling muds when drilling through salt formations or when drilling in the open sea, then protective colloids such as starch and starch derivatives, carboximethylhydroxiethyl-carboxymethyl celluloses, biopolymers and partially saponified acrylamides are necessary to stabilize these dispersions. At very high solids contents, low molecular weight ionic polymers are preferred. The use of additives for drilling fluids is very detailed in: George R. Gray, H.C.H. Darly, Walter F. Rogers "Composition and Properties of Oil Well Drilling Fluids, Fourth Edition, Gulf Publishing Company Houston / Texas 1980".

In letzter Zeit haben sich Mischpolymerisate aus Vinylsulfonat und Vinylamid gemäß DOS 2 931 897 und DAS 2 444 108 bei Einsatz in salinen Bohrspülungen zur Stabilisierung vorab eingestellter Eigenschaften in sehr tiefen heißen Bohrungen sehr gut bewährt.Recently, copolymers of vinyl sulfonate and vinyl amide in accordance with DOS 2 931 897 and DAS 2 444 108 have proven themselves very well when used in saline drilling fluids to stabilize pre-set properties in very deep hot holes.

In Zementschlämmen, die verpumpt werden, setzen Dispergiermittel die Viskosität herab. Dies erleichtert den Pumpvorgang und erlaubt es, den Wassergehalt zu reduzieren, was die mechanischen Eigenschaften des ausgehärteten Betons verbessert. In Zementschlämmen kommen Lignosulfonate, Polyacrylsäuren, Kondensationsprodukte aus Mononaphthalinsulfonaten und Formaldehyd gemäß US-PS 3 465 825 und N-sulfoalkylsubstituierte Acrylamide gemäß US-PS 4 053 323 als Dispergiermittel zum Einsatz. Je nach Anwendungsgebiet setzt man Zementschlämmen noch Wasserverlustreduzierer, Abbindeverzögerer oder auch Abbindebeschleuniger zu, die mit dem jeweiligen Dispergiermittel verträglich sein müssen. Dies schränkt die Verwendbarkeit der Dispergatortypen ein. So können z.B. beim Einsatz von Kalziumsalzen als Abbindebeschleuniger keine Polyacrylsäuren als Dispergatoren verwendet werden.In cement slurries that are pumped, dispersants reduce the viscosity. This facilitates the pumping process and allows the water content to be reduced, which improves the mechanical properties of the hardened concrete. Lignosulfonates, polyacrylic acids, condensation products of mononaphthalenesulfonates and formaldehyde according to US Pat. No. 3,465,825 and N-sulfoalkyl-substituted acrylamides according to US Pat. No. 4,053,323 are used as dispersants in cement slurries. Depending on the field of application, cement slurries are added with water loss reducers, setting retarders or setting accelerators, which must be compatible with the respective dispersant. This limits the usability of the dispersant types. For example, When using calcium salts as setting accelerators, no polyacrylic acids are used as dispersing agents.

Auch teilverseifte Polyacrylamide als Wasservelustreduzierer lassen in ihrer Wirkung in Gegenwart von Kalziumchlorid stark nach. Bei besonders hohen Belastungen der Dispersionen z.B. von Zementschlämmen und Bohrspülungen auf Basis Salzwasser für sehr tiefe und heiße Bohrungen, ist es schwierig, optimale Eigenschaften einzustellen. Bekannt ist auch die Verwendung von Copolymerisaten aus (Meth)acrylamidoalkyl- sulfonsäuren und (Meth) acrylamid als Bohrhilfsmittel (US-A4 293 427). Aus DE-B 2 444 108 ist zum gleichen Zweck die Verwendung eines Copolymerisats bekannt, das aus Vinyl- bzw. Alkylsulfonsäuren, (Meth) acrylamiden und N-Vinyl-N-alkyl-carbonamiden besteht.Partially saponified polyacrylamides as water void reducers also decrease significantly in their presence in the presence of calcium chloride. At particularly high loads on the dispersions e.g. cement slurries and drilling fluids based on salt water for very deep and hot drilling, it is difficult to set optimal properties. It is also known to use copolymers of (meth) acrylamidoalkylsulfonic acids and (meth) acrylamide as drilling aids (US-A4 293 427). For the same purpose, DE-B 2 444 108 discloses the use of a copolymer which consists of vinyl or alkylsulfonic acids, (meth) acrylamides and N-vinyl-N-alkylcarbonamides.

Weiterhin finden als Dispergiermittel die unterschiedlichsten nicht-, an- und kationischen Tenside Verwendung.A wide variety of non-, cationic and cationic surfactants are also used as dispersants.

Gegenstand der Erfindung ist die Verwendung von Copolymeren bestehend zu 5-95 Gew.-% aus (Meth) acrylsäure oder deren Ammonium- oderAIkali-salzen oder teilverseiftem (Meth)acrylamid und zu 5-95 Gew.-% aus Gruppen der Formel II, III, oder IV

Figure imgb0001
Figure imgb0002
Figure imgb0003
wobei R3 Wasserstoff, C1-Cs-Alkyl oder Phenyl und R4 ein Wasserstoffatom oder CH3 und R5 C1-C10-Alkylen und K+ Ammonium, Lithium, Natrium oder Kalium bedeuten, ausgenommen solche Copolymeren, die aus hydrolysiertem Acrylamid und 2-Acrylamido-2-methylpropansulfonsäure oder aus Acrylamid bzw. Acrylsäure und Ethylensulfonat bestehen, als Dispergiermittel in Zementschlämmen und Bohrspülungen.The invention relates to the use of copolymers consisting of 5-95% by weight of (meth) acrylic acid or its ammonium or alkali salts or partially saponified (meth) acrylamide and 5-95% by weight of groups of the formula II, III, or IV
Figure imgb0001
Figure imgb0002
Figure imgb0003
wherein R 3 is hydrogen, C 1 -C s -alkyl or phenyl and R 4 is a hydrogen atom or CH 3 and R 5 are C 1 -C 10 -alkylene and K + ammonium, lithium, sodium or potassium, with the exception of those copolymers consisting of hydrolyzed acrylamide and 2-acrylamido-2-methylpropanesulfonic acid or consist of acrylamide or acrylic acid and ethylene sulfonate, as a dispersant in cement slurries and drilling fluids.

Die Molgewichte der Mischpolymerisate liegen zwischen 2 000 und 6 Mio, vorzugsweise zwischen 10 000 und 500 000. Höhere Molgewichte benötigt man bei extremen Anforderungen an die Suspension, wie hohe Temperaturen und Salzgehalte sowie niedrige Wasserabgaben.The molecular weights of the copolymers are between 2,000 and 6 million, preferably between 10,000 and 500,000. Higher molecular weights are required in the event of extreme demands on the suspension, such as high temperatures and salinity levels and low water emissions.

Die Herstellung der zu verwendenden Copolymerisate kann in an sich bekannter Weise durch Umsetzung der Monomeren bei Temperaturen zwischen etwa -10 und + 80 °C, vorzugsweise bei 20 bis 60°C, in Gegenwart von geeigneten Polymerisationskatalysatoren vorgenommen werden. Die Polymerisation erfolgt zweckmäßig in wäßriger Phase, ggf. können jedoch auch wäßrige Lösungen von wassermischbaren organischen Lösungsmitteln, wie z.B. Methanol, Ethanol, tert. Butylalkohol, Tetrahydrofuran oder Dimethylformamid als Polymerisationsmedium dienen. Als Polymerisationskatalysatoren kommen vor allem Perverbindungen wie Benzoylperoxid, Acetylperoxid, tert. Butylhydroperoxid oder Alkali- und Ammoniumperoxiddisulfat oder auch Redox-Systeme wie N-p-Tolylsulfonylmethylcarbamidsäuremethylester/Ammoniumperoxiddisulfat, in Betracht.The copolymers to be used can be prepared in a manner known per se by reacting the monomers at temperatures between about -10 and + 80 ° C., preferably at 20 to 60 ° C., in the presence of suitable polymerization catalysts. The polymerization is expediently carried out in the aqueous phase; however, aqueous solutions of water-miscible organic solvents, such as e.g. Methanol, ethanol, tert. Butyl alcohol, tetrahydrofuran or dimethylformamide serve as the polymerization medium. Per-compounds such as benzoyl peroxide, acetyl peroxide, tert. Butyl hydroperoxide or alkali and ammonium peroxide disulfate or also redox systems such as N-p-tolylsulfonylmethylcarbamidic acid methyl ester / ammonium peroxide disulfate.

Gegebenenfalls kann auch der Zusatz von Cokatalysatoren wie Dibutylaminhydrochlorid oder Spuren von Kupfersalzen zweckmäßig sein. Als Polymerisations-Initiatoren können auch Verbindungen wie z.B. Diazoisobutyronitril zugesetzt werden.If appropriate, the addition of cocatalysts such as dibutylamine hydrochloride or traces of copper salts may also be appropriate. Compounds such as e.g. Diazoisobutyronitrile can be added.

Man verwendet vorzugsweise folgende Monomere für die Herstellung der zu verwendenden Mischpolymerisate:

  • 1. Acrylsäure
  • 2. Vinylsulfonsäure
  • 3. Methallylsulfonsäure
  • 4. Acrylamidopropenylmethylensulfonsäure.
The following monomers are preferably used for the preparation of the copolymers to be used:
  • 1. Acrylic acid
  • 2. Vinyl sulfonic acid
  • 3. Methallylsulfonic acid
  • 4. Acrylamidopropenylmethylene sulfonic acid.

Die Mischpolymrisate fallen als viskose, vorzugsweise wäßrige Lösungen an. Sie können in dieser Form verwendet werden. Ist es beabsichtigt, die Mischpolymerisate in fester Form herzustellen, dann können die Polymerisatlösungen einen Verdampfungs- oder Trockenprozeß, z.B. Sprüh- oder Walzentrocknung unterworfen werden. Für die Anwendung ist es sinnvoll, daß die Sulfogruppen in den Mischpolymerisaten in Form der Ammonium- oder Alkalisalze vorliegen.The mixed polymrisates are obtained as viscous, preferably aqueous solutions. They can be used in this form. If it is intended to prepare the copolymers in solid form, the polymer solutions can be subjected to an evaporation or drying process, e.g. Spray or roller drying. For the application, it makes sense that the sulfo groups are present in the copolymers in the form of the ammonium or alkali salts.

Die Mischpolymerisate wirken sehr effektiv dispergierend auf sehr geringe Mengen von Feststoffen, z.B. Calciumcarbonat in technischen Kühlkreisläufen von nur z.B. 10 ppm oder bei sehr feststoffreichen Zementschlämmen bis zu 80% Feststoffgehalt. In den Kühlwässern ist die minimale Einsatzkonzentration 5 ppm, während sie in den Zementschlämmen bis zu 20% betragen kann. Die hohen Konzentrationen in den Zementschlämmen verbessern merklich die mechanischen Eigenschaften des ausgehärteten Zements. Nur die sehr gute Dispergierwirkung der Mischpolymerisate ermöglicht es, die genannten hohen Konzentrationen dieser Polymeren im Zementschlamm homogen zu verteilen.The copolymers have a very effective dispersing effect on very small amounts of solids, e.g. Calcium carbonate in technical cooling circuits of only e.g. 10 ppm or up to 80% solids content in cement slurries with a high solids content. The minimum application concentration in the cooling water is 5 ppm, while it can be up to 20% in the cement slurry. The high concentrations in the cement slurries noticeably improve the mechanical properties of the hardened cement. Only the very good dispersing effect of the copolymers makes it possible to homogeneously distribute the high concentrations of these polymers mentioned in the cement slurry.

Beispiele:Examples: 1. Dispersion von Calciumcarbonat1. Dispersion of calcium carbonate

Benutzt wurde eine Aufschlämmung von frisch gefälltem Calciumcarbonat (100 mg/I) in Wasser. 500 ml dieser Aufschlämmung wurden in Meßzylindern 25, 100 und 500 ppm eines Mischpolymerisats, bestehend aus 10% Methallylsulfonsäure und 90% Acrylsäure zugesetzt (K-Wert ca. 30). Es wurde geschüttelt, ca. 2 Stunden stehengelassen, anschließend die oben stehende Menge Wasser (250 m3) dekantiert und der Feststoffgehalt darin bestimmt.

Figure imgb0004
Figure imgb0005
Figure imgb0006
A slurry of freshly precipitated calcium carbonate (100 mg / l) in water was used. 500 ml of this slurry were added in measuring cylinders 25, 100 and 500 ppm of a copolymer consisting of 10% methallylsulfonic acid and 90% acrylic acid (K value approx. 30). It was shaken for about 2 hours left to stand, then decant the above amount of water (250 m 3 ) and determine the solids content therein.
Figure imgb0004
Figure imgb0005
Figure imgb0006

Mischpolymerisat A:Copolymers A:

  • 90% Acrylsäure90% acrylic acid
  • 10% Na-Methallylsulfonat10% Na methallyl sulfonate
Mischpolymerisat B:Copolymers B:

  • 65% Acrylsäure65% acrylic acid
  • 35% Acrylamidopropenylmethylensulfonat35% acrylamidopropenylmethylene sulfonate

Die Bohrspülungen wurden bei 20°C und dann nach 15 Stunden Alterung bei 200°C gemessen. Der K-Wert der Polymere (Fikentscher, Cellulose-Chemie 13, 1932, S. 58) betrug bei den Polymeren ca. 60. Die scheinbare Viskosität und die Fließgrenze wurden mit dem FANN-Viskosimeter 35 SA gemessen. Der Wasserverlust nach API ist die Filtrationsrate in 30 Min. nach « API Code 29 » mit einer genormten Filterpresse bei 7 kg/cm2.The drilling fluids were measured at 20 ° C and then after aging for 15 hours at 200 ° C. The K value the polymer (Fikentscher, Cellulose-Chemie 13, 1932, p. 58) was approx. 60 for the polymers. The apparent viscosity and the yield point were measured with the FANN viscometer 35 SA. The water loss according to API is the filtration rate in 30 minutes according to «API Code 29» with a standardized filter press at 7 kg / cm 2 .

3. Zementschlämme3. cement slurry a. Zusammensetzung:a. Composition:

Figure imgb0007
Figure imgb0007

Die Einsatzmenge der Mischpolymerisate beträgt jeweils 0,75%. Scheinbare Viskosität und Fließgrenze wurden mit dem FANN-Viskosimeter 35 SA ermittelt.The amount of the copolymers used is 0.75% in each case. Apparent viscosity and yield point were determined with the FANN 35 SA viscometer.

b. Zusammensetzung:b. Composition:

Figure imgb0008
Figure imgb0008

4. Feststoffsuspension auf Basis Bariumsulfat, Gips, Kalziumkarbonat und Kohle.4. Solid suspension based on barium sulfate, gypsum, calcium carbonate and coal.

  • a) Bariumsulfat
    • Der Feststoffgehalt beträgt 80 Gew.-%,
    • die Dispergatorkonzentration 0,25 Gew.-%
    a) Barium sulfate
    • The solids content is 80% by weight,
    • the dispersant concentration 0.25% by weight
  • b) Gips: CaS04.2 H20
    • Der Feststoffgehalt beträgt 55 Gew.-%,
    • die Dispergatorkonzentration 1,0 Gew.-%
    b) Gypsum: CaS0 4 . 2 H20
    • The solids content is 55% by weight,
    • the dispersant concentration 1.0% by weight
  • c) Kalziumkarbonat
    • Der Feststoffgehalt beträgt 55 Gew.-%,
    • die Dispergatorkonzentration 0,25 Gew.-%
    c) calcium carbonate
    • The solids content is 55% by weight,
    • the dispersant concentration 0.25% by weight
  • d) Kohle
    • Der Feststoffgehalt beträgt 70 Gew.-%, die Dispergatorkonzentration 0,25 Gew.-%.
    d) coal
    • The solids content is 70% by weight, the dispersant concentration is 0.25% by weight.

Alle Versuche wurden mit einem Dispergator durchgeführt, der einen K-Wert von ca. 60 hatte und wie folgt zusammengesetzt war:

  • 65 Gew.-% Acrylsäure
  • 30 Gew.-% Acrylamidomethylenpropenylsulfonsäure
  • 5 Gew.-% Methylsulfonsäure
alle Monomere lagen als Natriumsalze vor.All tests were carried out with a disperser which had a K value of approx. 60 and was composed as follows:
  • 65% by weight acrylic acid
  • 30% by weight of acrylamidomethylene propenyl sulfonic acid
  • 5% by weight methylsulfonic acid
all monomers were in the form of sodium salts.

Claims (3)

1. The use of a copolymer comprising 5 - 95% by weight of ( meth ) acrylic acid or ammonium or alkali metal salts thereof or partly hydrolyzed ( meth ) acrylamide and of 5 - 95% by weight of groups of the formula II, III or IV
Figure imgb0010
in which R3 denotes hydrogen, C1-C6-alkyl or phenyl, R4 denotes a hydrogen atom or CH3, and R5 denotes Ci-C10-alkylene and K+ denotes ammonium, lithium, sodium or potassium, excluding those copolymers which consist of hydrolyzed acrylamide and 2-acrylamido-2-methylpropane-sulfonic acid or of acrylamide or acrylic acid and ethylene sulfonate, as dispersant in cement slurries and drilling muds.
2. A cement slurry or drilling mud which contains a copolymer as claimed in claim 1 in a concentration of 5 ppm to 20% by weight, preferably 10 ppm to 5% by weight.
3. A cement slurry or drilling mud as claimed in claim 2, which contains the solids to be dispersed in a concentration of 10 ppm to 80% by weight, preferably 50 ppm to 65% by weight.
EP84112373A 1983-10-22 1984-10-13 Hydrosoluble copolymers and their use as dispersants of solid matter Expired - Lifetime EP0141327B2 (en)

Priority Applications (1)

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AT84112373T ATE42757T1 (en) 1983-10-22 1984-10-13 WATER-SOLUBLE MIXED POLYMERS AND THEIR USE AS DISPERGATORS FOR SOLIDS.

Applications Claiming Priority (2)

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DE19833338431 DE3338431A1 (en) 1983-10-22 1983-10-22 WATER-SOLUBLE MIXED POLYMERS AND THE USE THEREOF AS DISPERGERS FOR SOLIDS
DE3338431 1983-10-22

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EP0141327B1 EP0141327B1 (en) 1989-05-03
EP0141327B2 true EP0141327B2 (en) 1992-08-19

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US4652623A (en) * 1984-11-23 1987-03-24 Calgon Corporation Polymers for use as filtration control aids in drilling muds
JPH0625317B2 (en) * 1986-08-26 1994-04-06 日本ペイント株式会社 Spherical collapsible vinyl resin particles for antifouling paint
JPH01226757A (en) * 1988-03-04 1989-09-11 Takemoto Oil & Fat Co Ltd Dispersing agent for cement
CA2081465A1 (en) * 1990-04-26 1991-10-27 James B. Bloys Dispersant compositions for subterranean well drilling and completion
US5221489A (en) * 1990-04-26 1993-06-22 Atlantic Richfield Company Sulfonated polymeric dispersant compositions for subterranean well drilling, completion, and cementing
DE4320220A1 (en) * 1993-06-18 1994-12-22 Basf Ag Use of polymers I which contain copolymerized special monoethylenically unsaturated sulfonic acids as auxiliaries in the spray drying of aqueous dispersions of polymers II
FR2732009B1 (en) * 1995-03-22 1997-06-06 Schlumberger Cie Dowell CEMENTING COMPOSITION COMPRISING A DISPERSING AGENT AND ITS APPLICATION TO CEMENTING OIL WELLS
DE19909231C2 (en) * 1999-03-03 2001-04-19 Clariant Gmbh Water-soluble copolymers based on AMPS and their use as drilling aids
CN1093095C (en) * 2000-11-07 2002-10-23 复旦大学 Efficient carboxilic acid grafting water-reducing agent and its synthesis
US7247662B2 (en) 2001-10-07 2007-07-24 Nippon Shokubai Co., Ltd. Cement dispersant, its production process, and cement composition using the cement dispersant
JP2008208016A (en) * 2007-02-28 2008-09-11 Nippon Shokubai Co Ltd Powdered cement dispersant
WO2017158441A1 (en) * 2016-03-17 2017-09-21 Lubrizol Oilfield Solutions, Inc. Carboxylic acid/acrylamidoalkane sulfonic acid/styrene sulfonate copolymers for ultrahigh temperature and pressure retardation of oil-well cement

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US3730900A (en) 1972-09-25 1973-05-01 Milchem Inc Composition and process for drilling subterranean wells
DE2444108C2 (en) 1974-09-14 1978-01-19 Hoechst Ag WATER-BASED CLAY FLUSHING FOR DEEP HOLES AND THE USE OF A MIXED POLYMERIZED FOR SUCH FLUSHING
US4053323A (en) 1976-11-11 1977-10-11 Calgon Corporation Method of using cementing composition having improved flow properties
US4293427A (en) * 1979-03-09 1981-10-06 Milchem Incorporated Drilling fluid containing a copolymer filtration control agent

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ES8506331A1 (en) 1985-07-01
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CA1258947A (en) 1989-08-29
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ATE42757T1 (en) 1989-05-15
AU583481B2 (en) 1989-05-04
NO844203L (en) 1985-04-23
JPS60104109A (en) 1985-06-08
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DE3338431A1 (en) 1985-05-02

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